TY - JOUR
T1 - Antifungal activity of chemical constituents from piper pesaresanum C. DC. and derivatives against phytopathogen fungi of cocoa
AU - Chitiva-Chitiva, Luis C.
AU - Ladino-Vargas, Cristóbal
AU - Cuca-Suárez, Luis E.
AU - Prieto-Rodríguez, Juliet A.
AU - Patiño-Ladino, Oscar J.
N1 - Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/6/1
Y1 - 2021/6/1
N2 - In this study, the antifungal potential of chemical constituents from Piper pesaresanum and some synthesized derivatives was determined against three phytopathogenic fungi associated with the cocoa crop. The methodology included the phytochemical study on the aerial part of P. pesaresanum, the synthesis of some derivatives and the evaluation of the antifungal activity against the fungi Moniliophthora roreri, Fusarium solani and Phytophthora sp. The chemical study allowed the isolation of three benzoic acid derivatives (1–3), one dihydrochalcone (4) and a mixture of sterols (5–7). Seven derivatives (8–14) were synthesized from the main constituents, of which compounds 9, 10, 12 and 14 are reported for the first time. Benzoic acid derivatives showed strong antifungal activity against M. roreri, of which 11 (3.0 ± 0.8 μM) was the most active compound with an IC50 lower compared with positive control Mancozeb® (4.9 ± 0.4 μM). Dihydrochalcones and acid derivatives were active against F. solani and Phytophthora sp., of which 3 (32.5 ± 3.3 μM) and 4 (26.7 ± 5.3 μM) were the most active compounds, respectively. The preliminary structure–activity relationship allowed us to establish that prenylated chains and the carboxyl group are important in the antifungal activity of benzoic acid derivatives. Likewise, a positive influence of the carbonyl group on the antifungal activity for dihydrochalcones was deduced.
AB - In this study, the antifungal potential of chemical constituents from Piper pesaresanum and some synthesized derivatives was determined against three phytopathogenic fungi associated with the cocoa crop. The methodology included the phytochemical study on the aerial part of P. pesaresanum, the synthesis of some derivatives and the evaluation of the antifungal activity against the fungi Moniliophthora roreri, Fusarium solani and Phytophthora sp. The chemical study allowed the isolation of three benzoic acid derivatives (1–3), one dihydrochalcone (4) and a mixture of sterols (5–7). Seven derivatives (8–14) were synthesized from the main constituents, of which compounds 9, 10, 12 and 14 are reported for the first time. Benzoic acid derivatives showed strong antifungal activity against M. roreri, of which 11 (3.0 ± 0.8 μM) was the most active compound with an IC50 lower compared with positive control Mancozeb® (4.9 ± 0.4 μM). Dihydrochalcones and acid derivatives were active against F. solani and Phytophthora sp., of which 3 (32.5 ± 3.3 μM) and 4 (26.7 ± 5.3 μM) were the most active compounds, respectively. The preliminary structure–activity relationship allowed us to establish that prenylated chains and the carboxyl group are important in the antifungal activity of benzoic acid derivatives. Likewise, a positive influence of the carbonyl group on the antifungal activity for dihydrochalcones was deduced.
KW - Benzoic acid derivatives
KW - Dihydrochalcones
KW - Fusarium solani
KW - Moniliophthora roreri
KW - Phytophthora sp
KW - Phytosanitary agents
KW - Piper pesaresanum
KW - Theobroma cacao
UR - http://www.scopus.com/inward/record.url?scp=85107340660&partnerID=8YFLogxK
U2 - 10.3390/molecules26113256
DO - 10.3390/molecules26113256
M3 - Article
C2 - 34071493
AN - SCOPUS:85107340660
SN - 1420-3049
VL - 26
JO - Molecules
JF - Molecules
IS - 11
M1 - 3256
ER -